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Distinct microbial and immune niches of the human colon.
James, Kylie R; Gomes, Tomas; Elmentaite, Rasa; Kumar, Nitin; Gulliver, Emily L; King, Hamish W; Stares, Mark D; Bareham, Bethany R; Ferdinand, John R; Petrova, Velislava N; Polanski, Krzysztof; Forster, Samuel C; Jarvis, Lorna B; Suchanek, Ondrej; Howlett, Sarah; James, Louisa K; Jones, Joanne L; Meyer, Kerstin B; Clatworthy, Menna R; Saeb-Parsy, Kourosh; Lawley, Trevor D; Teichmann, Sarah A.
Afiliación
  • James KR; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. kj7@sanger.ac.uk.
  • Gomes T; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Elmentaite R; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Kumar N; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Gulliver EL; Department of Molecular and Translational Sciences, Monash University, Clayton, Victoria, Australia.
  • King HW; Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.
  • Stares MD; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Bareham BR; Department of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge, UK.
  • Ferdinand JR; Molecular Immunity Unit, Department of Medicine, University of Cambridge, MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Petrova VN; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Polanski K; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Forster SC; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Jarvis LB; Department of Molecular and Translational Sciences, Monash University, Clayton, Victoria, Australia.
  • Suchanek O; Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
  • Howlett S; Department of Haematology, Clifford Allbutt Building, Cambridge, UK.
  • James LK; Molecular Immunity Unit, Department of Medicine, University of Cambridge, MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Jones JL; Department of Haematology, Clifford Allbutt Building, Cambridge, UK.
  • Meyer KB; Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.
  • Clatworthy MR; Department of Haematology, Clifford Allbutt Building, Cambridge, UK.
  • Saeb-Parsy K; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Lawley TD; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Teichmann SA; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Nat Immunol ; 21(3): 343-353, 2020 03.
Article en En | MEDLINE | ID: mdl-32066951
Gastrointestinal microbiota and immune cells interact closely and display regional specificity; however, little is known about how these communities differ with location. Here, we simultaneously assess microbiota and single immune cells across the healthy, adult human colon, with paired characterization of immune cells in the mesenteric lymph nodes, to delineate colonic immune niches at steady state. We describe distinct helper T cell activation and migration profiles along the colon and characterize the transcriptional adaptation trajectory of regulatory T cells between lymphoid tissue and colon. Finally, we show increasing B cell accumulation, clonal expansion and mutational frequency from the cecum to the sigmoid colon and link this to the increasing number of reactive bacterial species.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colon / Microbioma Gastrointestinal Límite: Adult / Humans Idioma: En Revista: Nat Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colon / Microbioma Gastrointestinal Límite: Adult / Humans Idioma: En Revista: Nat Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2020 Tipo del documento: Article